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FDA 510(k) Applications Submitted by VUNO Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231398
05/15/2023
VUNO Med-DeepBrain
VUNO Inc.
K241439
05/21/2024
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage
Vuno Inc.
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